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6505-01-166-3799

20 Products

SULF-10

SULFACETAMIDE SODIUM OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011663799

NSN

6505-01-166-3799

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SULF-10

SULFACETAMIDE SODIUM OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011663799

NSN

6505-01-166-3799

MFG

COOPER LABORATORIES INC COOPER VISION PHARMACEUTICALS INC DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V SULFACETAMIDE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: OPHTHALMIC
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 MILLILITERS
PRIMARY CONTAINER TYPE: TUBE WITH OPHTHALMIC TIP, COLLAPSIBLE
TOTAL PRIMARY CONTAINER QUANTITY: 12

C-1/2

CALCIUM ACETATE FOR INJECTION

NSN, MFG P/N

6505011664385

NSN

6505-01-166-4385

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C-1/2

CALCIUM ACETATE FOR INJECTION

NSN, MFG P/N

6505011664385

NSN

6505-01-166-4385

MFG

ORGANON INC ORGANON TEKNIKA CORP SUB OF AKZONE INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.300 GRAMS CALCIUM ACETATE ACTIVE INGREDIENT
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 5.300 GRAMS
PRIMARY CONTAINER TYPE: PACKET
TOTAL PRIMARY CONTAINER QUANTITY: 50

0069682

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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0069682

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

ASSOCIATION PHARMACEUTIQUE BELGE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

NDC00364-3040-53

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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NDC00364-3040-53

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

SCHEIN PHARMACEUTICAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

NDC11980-0260-25

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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NDC11980-0260-25

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

ALLERGAN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

NDC24208-0540-05

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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NDC24208-0540-05

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

BAUSCH & LOMB PHARMACEUTICALS DIV BAUSCH & LOMB PHAMACEUTICAL

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

NDC61314-0235-05

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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NDC61314-0235-05

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

FALCON PHARMACEUTICALS LTD

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

PROPINE

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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PROPINE

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

ALLERGAN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

PROPINE COLLYRE 0.1/5ML

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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PROPINE COLLYRE 0.1/5ML

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

ALLERGAN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

S01EA02

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

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S01EA02

DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION,USP

NSN, MFG P/N

6505011664386

NSN

6505-01-166-4386

MFG

WHO COLLABORATING CENTRE FOR DRUG STATISTICS METHODOLOGY NORWEGIAN INSTITUTE OF PIBLIC HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DIPIVEFRIN HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DIPIVEFRIN HYDROCHLORIDE OPHTHALMIC SOLUTION USP 5ML BT
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP

12-815

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505011664390

NSN

6505-01-166-4390

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12-815

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505011664390

NSN

6505-01-166-4390

MFG

COBE LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 3.250 MILLIEQUIVALENTS CALCIUM ION PER LITER AND 103.250 MILLIEQUIVALENTS CHLORIDE ION PER LITER AND 137.500 MILLIEQUIVALENTS SODIUM ION PER LITER AND 39.250 MILLIEQUIVALENTS ACETATE ION PER LITER AND 0.750 MILLIEQUIVALENTS MAGNESIUM ION PER LITER AND
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 GALLONS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: STRENGTHS IN PAC AKJA ARE AFTER DILUTION WITH 34 PARTS WATER
TOTAL PRIMARY CONTAINER QUANTITY: 4
~1: 1.000 MILLIEQUIVALENTS POTASSIUM ION PER LITER

ACETATE RENALYTE

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505011664390

NSN

6505-01-166-4390

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ACETATE RENALYTE

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505011664390

NSN

6505-01-166-4390

MFG

COBE LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 3.250 MILLIEQUIVALENTS CALCIUM ION PER LITER AND 103.250 MILLIEQUIVALENTS CHLORIDE ION PER LITER AND 137.500 MILLIEQUIVALENTS SODIUM ION PER LITER AND 39.250 MILLIEQUIVALENTS ACETATE ION PER LITER AND 0.750 MILLIEQUIVALENTS MAGNESIUM ION PER LITER AND
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 GALLONS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: STRENGTHS IN PAC AKJA ARE AFTER DILUTION WITH 34 PARTS WATER
TOTAL PRIMARY CONTAINER QUANTITY: 4
~1: 1.000 MILLIEQUIVALENTS POTASSIUM ION PER LITER

NDC00054-8529-04

LITHIUM CITRATE SYRUP,USP

NSN, MFG P/N

6505011666610

NSN

6505-01-166-6610

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NDC00054-8529-04

LITHIUM CITRATE SYRUP,USP

NSN, MFG P/N

6505011666610

NSN

6505-01-166-6610

MFG

BOEHRINGER INGELHEIM ROXANE INC. DIV SUB OF BOEHRINGER INGELHEIM CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.600 MILLIEQUIVALENTS LITHIUM ION PER 5 MILLILITERS
ADMINISTRATION: ORAL
FLAVOR: RASPBERRY
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: CUP, UNIT DOSE
SPECIAL FEATURES: SUGAR FREE
TOTAL PRIMARY CONTAINER QUANTITY: 100

4084

ANTIVENIN,LATRODECTUS MACTANS,USP

NSN, MFG P/N

6505011667821

NSN

6505-01-166-7821

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4084

ANTIVENIN,LATRODECTUS MACTANS,USP

NSN, MFG P/N

6505011667821

NSN

6505-01-166-7821

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIVENIN LATRADECTUS MACTANS USP CRYSTALLINE POWDER SINGLE DOSE VIAL
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
IMMEDIATE CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: NON-PYROGENIC,CRYSTALLINE POWDER,SINGLE DOSE VIAL CONTAINING NOT LESS THAN 6000 ANTIVENIN UNITS,1 SUCH VIAL SHALL BE PACKAGED TOGETHER WITH A 1 ML VIAL OF NORMAL HORSE SERUM AND A 2.5 ML VIAL OF STERILE DILUENT FOR INJECTION
UNIT PACKAGE QUANTITY: 2
UNIT PACKAGE TYPE: PACKAGE

ANTIVENIN-SPIDER

ANTIVENIN,LATRODECTUS MACTANS,USP

NSN, MFG P/N

6505011667821

NSN

6505-01-166-7821

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ANTIVENIN-SPIDER

ANTIVENIN,LATRODECTUS MACTANS,USP

NSN, MFG P/N

6505011667821

NSN

6505-01-166-7821

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIVENIN LATRADECTUS MACTANS USP CRYSTALLINE POWDER SINGLE DOSE VIAL
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
IMMEDIATE CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: NON-PYROGENIC,CRYSTALLINE POWDER,SINGLE DOSE VIAL CONTAINING NOT LESS THAN 6000 ANTIVENIN UNITS,1 SUCH VIAL SHALL BE PACKAGED TOGETHER WITH A 1 ML VIAL OF NORMAL HORSE SERUM AND A 2.5 ML VIAL OF STERILE DILUENT FOR INJECTION
UNIT PACKAGE QUANTITY: 2
UNIT PACKAGE TYPE: PACKAGE

NDC00006-4084-00

ANTIVENIN,LATRODECTUS MACTANS,USP

NSN, MFG P/N

6505011667821

NSN

6505-01-166-7821

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NDC00006-4084-00

ANTIVENIN,LATRODECTUS MACTANS,USP

NSN, MFG P/N

6505011667821

NSN

6505-01-166-7821

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIVENIN LATRADECTUS MACTANS USP CRYSTALLINE POWDER SINGLE DOSE VIAL
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
IMMEDIATE CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: NON-PYROGENIC,CRYSTALLINE POWDER,SINGLE DOSE VIAL CONTAINING NOT LESS THAN 6000 ANTIVENIN UNITS,1 SUCH VIAL SHALL BE PACKAGED TOGETHER WITH A 1 ML VIAL OF NORMAL HORSE SERUM AND A 2.5 ML VIAL OF STERILE DILUENT FOR INJECTION
UNIT PACKAGE QUANTITY: 2
UNIT PACKAGE TYPE: PACKAGE

NDC00067-0200-68

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

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NDC00067-0200-68

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

MFG

AVENTIS PHARMACEUTICALS PRODUCTS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS THEOPHYLLINE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: THEOPHYLLINE EXTENDED-RELEASE CAPSULES USP 200MG 100S BT
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: ANHYDROUS
THERAPEUTIC EQUIVALENT: SLO-BID GYROCAPS BY RORER PHARMACEUTICAL

NDC00075-0200-00

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

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NDC00075-0200-00

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

MFG

AVENTIS PHARMACEUTICALS PRODUCTS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS THEOPHYLLINE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: THEOPHYLLINE EXTENDED-RELEASE CAPSULES USP 200MG 100S BT
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: ANHYDROUS
THERAPEUTIC EQUIVALENT: SLO-BID GYROCAPS BY RORER PHARMACEUTICAL

NDC00258-3634-01

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

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NDC00258-3634-01

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

MFG

INWOOD LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS THEOPHYLLINE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: THEOPHYLLINE EXTENDED-RELEASE CAPSULES USP 200MG 100S BT
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: ANHYDROUS
THERAPEUTIC EQUIVALENT: SLO-BID GYROCAPS BY RORER PHARMACEUTICAL

NDC00603-5951-21

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

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NDC00603-5951-21

THEOPHYLLINE EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505011668989

NSN

6505-01-166-8989

MFG

GENERICS BIDCO I LLC DBA QUALITEST PHARMACEUTICALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS THEOPHYLLINE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: THEOPHYLLINE EXTENDED-RELEASE CAPSULES USP 200MG 100S BT
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: ANHYDROUS
THERAPEUTIC EQUIVALENT: SLO-BID GYROCAPS BY RORER PHARMACEUTICAL